Home NDC 59321-056 ULTRA STRENGTH ZHENG GU SHUI
Product NDC 59321-056
11-digit product format 593210056
Labeler code 59321
Product ID 59321-056_39ee8407-942b-cb0f-e063-6394a90a20ad
Type HUMAN OTC DRUG
Nonproprietary name MENTHOL AND CAMPHOR
Dosage form LINIMENT
Route PERCUTANEOUS
Labeler GUANGXI YULIN PHARMACEUTICAL GROUP CO LTD
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-04-04
Marketing end 2028-05-01
Substance CAMPHOR (SYNTHETIC); MENTHOL
Active strength 4.1; 4.1 g/100mL; g/100mL
NDC exclude flag No
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base ULTRA STRENGTH ZHENG GU SHUI Active Ingredients# Ingredient, Strength table Ingredient Strength CAMPHOR (SYNTHETIC) 4.1 g/100mL MENTHOL 4.1 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 5TJD82A1ET Internal UNII lookup L7T10EIP3A Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 59321-056-02 ULTRA STRENGTH ZHENG GU SHUI 88 mL in 1 BOTTLE, WITH APPLICATOR LINIMENT 88 3 59321-056-02 ULTRA STRENGTH ZHENG GU SHUI 1 in 1 BOX LINIMENT 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59321-056 ULTRA STRENGTH ZHENG GU SHUI (MENTHOL AND CAMPHOR) LINIMENT [GUANGXI YULIN PHARMACEUTICAL GROUP CO LTD] 2 Current NDC, 2 package rows 20241127_53397663-044d-4e48-989b-2c6257af5f84.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 109 of 153 · 3,057 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 59321-056-02 59321005602 1 BOTTLE, WITH APPLICATOR in 1 BOX (59321-056-02) / 88 mL in 1 BOTTLE, WITH APPLICATOR 2023-04-04 2028-05-01 No No Historical